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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
0801708
In Commercial Distribution

  • B58208017080 ()
0801708

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
0801707
In Commercial Distribution

  • B58208017070 ()
0801707

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80161
In Commercial Distribution

  • B5820801610 ()
80161

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80160
In Commercial Distribution

  • B5820801600 ()
80160

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80159
In Commercial Distribution

  • B5820801590 ()
80159

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80158
In Commercial Distribution

  • B5820801580 ()
80158

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80157
In Commercial Distribution

  • B5820801570 ()
80157

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80156
In Commercial Distribution

  • B5820801560 ()
80156

  • Hand-held surgical retractor, reusable
RETRACTOR, ALL TYPES
GEORGE TIEMANN & CO.
80155
In Commercial Distribution

  • B5820801550 ()
80155

  • Hand-held surgical retractor, reusable
ELEVATOR, SURGICAL, GENERAL & PLASTIC SURGERY
GEORGE TIEMANN & CO.
08015321
In Commercial Distribution

  • B582080153210 ()
08015321

  • Bone lever/elevator, reusable
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